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发育中的鸡胚卵巢中用于RT-qPCR分析的内参基因的选择

Selection of reference genes for RT-qPCR analysis in developing chicken embryonic ovary.

作者信息

Wang Yi, Zhang Yu-Qing, Wu Zi-Wei, Fang Ting, Wang Fang, Zhao Han, Du Zhi-Qiang, Yang Cai-Xia

机构信息

College of Animal Science, Yangtze University, 434025, Jingzhou, Hubei, China.

出版信息

Mol Biol Rep. 2023 Apr;50(4):3379-3387. doi: 10.1007/s11033-023-08280-0. Epub 2023 Feb 2.

Abstract

BACKGROUND

Normalization of the expression profiling of target genes, in a tissue-specific manner and under different experimental conditions, requires stably expressed gene(s) to be used as internal reference(s). However, to study the molecular regulation of oocyte meiosis initiation during ovary development in chicken embryos, stable reference gene(s) still need to be compared and confirmed.

METHODS AND RESULTS

Six candidate genes previously used as internal references for the chicken embryo (Actb, Cvh, Dazl, Eef1a, Gapdh and Rpl15) were chosen, and their expression profiles in left ovaries dissected at five chicken embryonic days (E12.5, E15.5, E17.5, E18.5 and E20.5) were evaluated, respectively. Separately, GeNorm, NormFinder, BestKeeper and Comparative ΔCt methods were used to assess the stability of candidate reference genes, and all results were combined to give the final rank by RefFinder. All methods identified that Eef1a and Rpl15 were the two most stable internal reference genes, whereas Cvh is the most unstable one. Moreover, expression levels of three marker genes for chicken oocyte meiosis entry (Stra8, Scp3 and Dmc1) were normalized, based on Eef1a, Rpl15, or their combinations, respectively.

CONCLUSION

Our findings provide the most suitable internal reference genes (Eef1a and Rpl15), to investigate further molecular regulation of ovary development and oocyte meiosis initiation in chicken embryos.

摘要

背景

以组织特异性方式并在不同实验条件下使靶基因的表达谱标准化,需要使用稳定表达的基因作为内参。然而,为了研究鸡胚卵巢发育过程中卵母细胞减数分裂起始的分子调控,仍需要比较和确认稳定的参考基因。

方法与结果

选择了六个先前用作鸡胚内参的候选基因(Actb、Cvh、Dazl、Eef1a、Gapdh和Rpl15),并分别评估了它们在五个鸡胚日(E12.5、E15.5、E17.5、E18.5和E20.5)解剖的左侧卵巢中的表达谱。另外,使用GeNorm、NormFinder、BestKeeper和比较ΔCt方法评估候选参考基因的稳定性,并将所有结果合并以通过RefFinder给出最终排名。所有方法均确定Eef1a和Rpl15是两个最稳定的内参基因,而Cvh是最不稳定的。此外,分别基于Eef1a、Rpl15或它们的组合,对鸡卵母细胞减数分裂进入的三个标记基因(Stra8、Scp3和Dmc1)的表达水平进行了标准化。

结论

我们的研究结果提供了最合适的内参基因(Eef1a和Rpl15),以进一步研究鸡胚卵巢发育和卵母细胞减数分裂起始的分子调控。

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